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A cyclodextrin molecular reactor for the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles

Barr, Lorna; Lincoln, Stephen F; Easton, Christopher

Description

6A-Deoxy-6A-propynamido-β-cyclodextrin reacts with 4-tert-butylphenyl azide in aqueous solution, to form the 5-(aminocarbonyl)-substituted triazole in preference to the 4-(aminocarbonyl)- substituted analogue, in a ratio of 25:1. The cyclodextrin moiety

dc.contributor.authorBarr, Lorna
dc.contributor.authorLincoln, Stephen F
dc.contributor.authorEaston, Christopher
dc.date.accessioned2015-12-13T22:35:19Z
dc.identifier.issn1061-0278
dc.identifier.urihttp://hdl.handle.net/1885/76535
dc.description.abstract6A-Deoxy-6A-propynamido-β-cyclodextrin reacts with 4-tert-butylphenyl azide in aqueous solution, to form the 5-(aminocarbonyl)-substituted triazole in preference to the 4-(aminocarbonyl)- substituted analogue, in a ratio of 25:1. The cyclodextrin moiety
dc.publisherTaylor & Francis Group
dc.sourceSupramolecular Chemistry
dc.subjectKeywords: Cycloadditions; Cyclodextrins; Molecular reactors; Regio selectivity; Templates; Triazoles
dc.titleA cyclodextrin molecular reactor for the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles
dc.typeJournal article
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.citationvolume17
dc.date.issued2005
local.identifier.absfor030302 - Nanochemistry and Supramolecular Chemistry
local.identifier.ariespublicationMigratedxPub5349
local.type.statusPublished Version
local.contributor.affiliationBarr, Lorna, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationLincoln, Stephen F, University of Adelaide
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.description.embargo2037-12-31
local.bibliographicCitation.issue7
local.bibliographicCitation.startpage547
local.bibliographicCitation.lastpage555
local.identifier.doi10.1080/10610270500329131
dc.date.updated2015-12-11T09:27:13Z
local.identifier.scopusID2-s2.0-30344441790
CollectionsANU Research Publications

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